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FDA 510(k)

ESCORT-LINK ARRHYTHMIA OPTION 23L

K-Number: K915153 · 1992-04-27

ApplicantMedical Data Electronics
Decision Date1992-04-27
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESCORT-LINK ARRHYTHMIA OPTION 23L is the device name listed in this FDA 510(k) record. The listed applicant is Medical Data Electronics. It received FDA 510(k) clearance on 1992-04-27 under 510(k) number K915153. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESCORT-LINK ARRHYTHMIA OPTION 23L?

ESCORT-LINK ARRHYTHMIA OPTION 23L is a medical device that received FDA 510(k) clearance on 1992-04-27. The listed applicant is Medical Data Electronics. The 510(k) number is K915153.

When did ESCORT-LINK ARRHYTHMIA OPTION 23L receive FDA 510(k) clearance?

ESCORT-LINK ARRHYTHMIA OPTION 23L received FDA 510(k) clearance on 1992-04-27, under 510(k) number K915153.

Who is the listed applicant for ESCORT-LINK ARRHYTHMIA OPTION 23L?

The FDA 510(k) record lists Medical Data Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESCORT-LINK ARRHYTHMIA OPTION 23L?

The FDA product code for ESCORT-LINK ARRHYTHMIA OPTION 23L is DSI.

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Other records listing Medical Data Electronics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K014294MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414K012336MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500K000660ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413K992413ESCORT 100/300 SERIES B (ESCORT II) PATIENT MONITORK992411ESCORT II+ 400 SERIES (ESCORT PRISM) MONITORK982104ESCORT-LINK CENTRAL STATION MONITOR MODEL 20500

View all 27 devices →

Related Devices (Code: DSI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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